LENS 4K Camera Head 72205058

GUDID 00885556720790

LENS 4K A/C CAMERA HEAD

Smith & Nephew, Inc.

Camera control unit

• Primary Device ID: 00885556720790
• NIH Device Record Key: 412c34c6-ed17-48ea-b7c9-4d7e07a203d3
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LENS 4K Camera Head
• Version Model Number: 72205058
• Catalog Number: 72205058
• Company DUNS: 109903521
• Company Name: Smith & Nephew, Inc.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Unsafe
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: false
• Serial Number: true
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM

Device Identifiers

Device Issuing Agency	Device ID
GS1	00885556720790 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K191177

FDA Product Code

• GCJ: Laparoscope, general & plastic surgery

Sterilization

• Steralize Prior To Use: true
• Device Is Sterile: false

[00885556720790]

Liquid Chemical;Moist Heat or Steam Sterilization

[00885556720790]

Liquid Chemical;Moist Heat or Steam Sterilization

[00885556720790]

Liquid Chemical;Moist Heat or Steam Sterilization

[00885556720790]

Liquid Chemical;Moist Heat or Steam Sterilization

[00885556720790]

Liquid Chemical;Moist Heat or Steam Sterilization

[00885556720790]

Liquid Chemical;Moist Heat or Steam Sterilization

[00885556720790]

Liquid Chemical;Moist Heat or Steam Sterilization

[00885556720790]

Liquid Chemical;Moist Heat or Steam Sterilization

[00885556720790]

Liquid Chemical;Moist Heat or Steam Sterilization

[00885556720790]

Liquid Chemical;Moist Heat or Steam Sterilization

[00885556720790]

Liquid Chemical;Moist Heat or Steam Sterilization

[00885556720790]

Liquid Chemical;Moist Heat or Steam Sterilization

[00885556720790]

Liquid Chemical;Moist Heat or Steam Sterilization

[00885556720790]

Liquid Chemical;Moist Heat or Steam Sterilization

[00885556720790]

Liquid Chemical;Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2019-09-26
• Device Publish Date: 2019-09-18

Devices Manufactured by Smith & Nephew, Inc.

• 23596010587682 - FOOTPRINT: 2025-01-10 REPLACEMENT END CAPS FOR MALLET SET OF 2
• 00885556905463 - NA: 2024-12-25 INSERT TRIAL PITCHFORK
• 00885556915288 - NA: 2024-12-25 LM/RL TIBIA ALIGNMENT GUIDE SHORT
• 00885556921517 - Trigen: 2024-12-10 Swivel Guide Bolt Wrench
• 00885556921388 - Legion: 2024-12-04 Legion AP Cutting Block - Size 8
• 00885556921395 - Legion: 2024-12-04 Legion AP Cutting Block - Size 7
• 00885556921401 - Legion: 2024-12-04 Legion AP Cutting Block - Size 6
• 00885556921418 - Legion: 2024-12-04 Legion AP Cutting Block - Size 5